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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179051Generated: November 3, 2026

Acetic Acid → HCID 10110019, compound

https://huagongshe.com/reaction/1179051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(+-)-alpha-MethyltryptamineHCID 9287—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 10110019HCID 1011001917%

Reaction Steps

DL-α-Methyltryptamine (348 mg, 2 mmol) was dissolved in dry 1,2-dichloroethane (10 ml) under argon. After addition of 4-dimethylamino-4-phenylcyclohexanone (435 mg) and glacial acetic acid (229 μl), the mixture was stirred for one hour at RT. Sodium triacetoxyborohydride (550 mg) was then added and the suspension was stirred for four days at RT. For working up, water (15 ml) was added to the reaction mixture. The clear phases were separated and the aqueous phase was washed with ether (10 ml) and then rendered strongly alkaline with sodium hydroxide solution. The aqueous phase was extracted with ethyl acetate (4×10 ml), the combined extracts were dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product obtained (723 mg) was recrystallized twice from a mixture of ethyl acetate/cyclohexane (2 ml/6 ml). A fraction of the nonpolar diastereoisomer of N′-[2-(1H-indol-3-yl)-1-methyl-ethyl]-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine (128 mg, m.p. 155-162° C.) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-f98cf71803a64f4aac4bc9c403bfe4b8
Source noteuspto-grants-2007_10